Canonical Allele Identifier: CA2466659052

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154367873G= , CM000685.2:g.154367873G=	GRCh38
NC_000023.10:g.153596241G= , CM000685.1:g.153596241G=	GRCh37
NC_000023.9:g.153249435G=	NCBI36
NG_011506.1:g.11766C=
NG_011506.2:g.11766C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.591C=	ENSP00000353467.4:p.Ala197=
ENST00000369850.10:c.591C= MANE Select	ENSP00000358866.3:p.Ala197=
ENST00000369856.8:c.510C=	ENSP00000358872.4:p.Ala170=
ENST00000422373.6:c.591C=	ENSP00000416926.2:p.Ala197=
ENST00000610817.5:c.591C=	ENSP00000480593.2:p.Ala197=
ENST00000676696.1:c.591C=	ENSP00000503392.1:p.Ala197=
ENST00000344736.8:c.591C=	ENSP00000358863.3:p.Ala197=
ENST00000360319.8:c.591C=	ENSP00000353467.4:p.Ala197=
ENST00000369850.7:c.591C=	ENSP00000358866.3:p.Ala197=
ENST00000369856.7:c.510C=	ENSP00000358872.4:p.Ala170=
ENST00000420627.5:c.549C=	ENSP00000408921.1:p.Ala183=
ENST00000422373.5:c.591C=	ENSP00000416926.1:p.Ala197=
ENST00000610817.4:c.510C=	ENSP00000480593.1:p.Ala170=
NM_001110556.1:c.591C=	NP_001104026.1:p.Ala197=
NM_001456.3:c.591C=	NP_001447.2:p.Ala197=
XM_011531127.1:c.591C=	XP_011529429.1:p.Ala197=
XM_011531128.1:c.591C=	XP_011529430.1:p.Ala197=
XM_011531129.1:c.591C=	XP_011529431.1:p.Ala197=
XM_011531130.1:c.591C=	XP_011529432.1:p.Ala197=
XM_011531131.1:c.591C=	XP_011529433.1:p.Ala197=
NM_001110556.2:c.591C= MANE Select	NP_001104026.1:p.Ala197=
NM_001456.4:c.591C=	NP_001447.2:p.Ala197=